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Items: 1 to 20 of 44

1.
The Histone Fold Subunits of Drosophila CHRAC Facilitate Nucleosome Sliding through Dynamic DNA Interactions
Klaus F. Hartlepp, Carlos Fernández-Tornero, Anton Eberharter, Tim Grüne, Christoph W. Müller, Peter B. Becker
Mol Cell Biol. 2005 Nov; 25(22): 9886–9896. doi: 10.1128/MCB.25.22.9886-9896.2005
PMCID:
PMC1280263
AbstractArticlePDF–633K
2.
The DNA chaperone HMGB1 facilitates ACF/CHRAC-dependent nucleosome sliding
Tiziana Bonaldi, Gernot Längst, Ralf Strohner, Peter B. Becker, Marco E. Bianchi
EMBO J. 2002 Dec 16; 21(24): 6865–6873. doi: 10.1093/emboj/cdf692
PMCID:
PMC139112
AbstractArticlePDF–226K
3.
Acf1, the largest subunit of CHRAC, regulates ISWI-induced nucleosome remodelling
Anton Eberharter, Simona Ferrari, Gernot Längst, Tobias Straub, Axel Imhof, Patrick Varga-Weisz, Matthias Wilm, Peter B. Becker
EMBO J. 2001 Jul 16; 20(14): 3781–3788. doi: 10.1093/emboj/20.14.3781
PMCID:
PMC125259
AbstractArticlePDF–217K
4.
Two histone fold proteins, CHRAC-14 and CHRAC-16, are developmentally regulated subunits of chromatin accessibility complex (CHRAC)
Davide F.V. Corona, Anton Eberharter, Andreja Budde, Renate Deuring, Simona Ferrari, Patrick Varga-Weisz, Matthias Wilm, John Tamkun, Peter B. Becker
EMBO J. 2000 Jun 15; 19(12): 3049–3059. doi: 10.1093/emboj/19.12.3049
PMCID:
PMC203371
AbstractArticlePDF–710K
5.
Association of Mutations in Replicative DNA Polymerase Genes with Human Disease: Possible Application of Drosophila Models for Studies
Masamitsu Yamaguchi, Sue Cotterill
Int J Mol Sci. 2023 May; 24(9): 8078. Published online 2023 Apr 29. doi: 10.3390/ijms24098078
PMCID:
PMC10178534
AbstractArticlePDF–857K
6.
Ras-ERK-ETS inhibition alleviates neuronal mitochondrial dysfunction by reprogramming mitochondrial retrograde signaling
Olivia F. Duncan, Lucy Granat, Ramya Ranganathan, Vandana K. Singh, David Mazaud, Manolis Fanto, David Chambers, Clive G. Ballard, Joseph M. Bateman
PLoS Genet. 2018 Jul; 14(7): e1007567. Published online 2018 Jul 30. doi: 10.1371/journal.pgen.1007567
PMCID:
PMC6085068
AbstractArticlePDF–21M
7.
A Metazoan ATAC Acetyltransferase Subunit That Regulates Mitogen-activated Protein Kinase Signaling Is Related to an Ancient Molybdopterin Synthase Component
Tamaki Suganuma, Arcady Mushegian, Selene K. Swanson, Laurence Florens, Michael P. Washburn, Jerry L. Workman
Mol Cell Proteomics. 2012 May; 11(5): 90–99. Published online 2012 Feb 18. doi: 10.1074/mcp.M111.015818
PMCID:
PMC3418850
AbstractArticlePDF–673K
8.
The DNA polymerases of Drosophila melanogaster
Steven J. Marygold, Helen Attrill, Elena Speretta, Kate Warner, Michele Magrane, Maria Berloco, Sue Cotterill, Mitch McVey, Yikang Rong, Masamitsu Yamaguchi
Fly (Austin) 2020; 14(1-4): 49–61. Published online 2020 Jan 14. doi: 10.1080/19336934.2019.1710076
PMCID:
PMC7714529
AbstractArticlePDF–1.9M
9.
Kinetochore-independent mechanisms of sister chromosome separation
Hannah Vicars, Travis Karg, Brandt Warecki, Ian Bast, William Sullivan
PLoS Genet. 2021 Jan; 17(1): e1009304. Published online 2021 Jan 29. doi: 10.1371/journal.pgen.1009304
PMCID:
PMC7886193
AbstractArticlePDF–2.8M
10.
The metazoan ATAC and SAGA coactivator HAT complexes regulate different sets of inducible target genes
Zita Nagy, Anne Riss, Sally Fujiyama, Arnaud Krebs, Meritxell Orpinell, Pascal Jansen, Adrian Cohen, Henk G. Stunnenberg, Shigeaki Kato, Làszlò Tora
Cell Mol Life Sci. 2010 Feb; 67(4): 611–628. Published online 2009 Nov 21. doi: 10.1007/s00018-009-0199-8
PMCID:
PMC11115597
AbstractArticlePDF–816K
11.
Exposure to the environmental pollutant bisphenol A diglycidyl ether (BADGE) causes cell over-proliferation in Drosophila
Michael J. Williams, Hao Cao, Therese Lindkvist, Tobias J. Mothes, Helgi B. Schiöth
Environ Sci Pollut Res Int. 2020; 27(20): 25261–25270. Published online 2020 Apr 28. doi: 10.1007/s11356-020-08899-7
PMCID:
PMC7329772
AbstractArticlePDF–2.1M
12.
Identification of E2F target genes that are rate limiting for dE2F1-dependent cell proliferation
Anabel Herr, Michelle Longworth, Jun-Yuan Ji, Michael Korenjak, David M. MacAlpine, Nicholas J. Dyson
Dev Dyn. Author manuscript; available in PMC 2013 Nov 1.
Published in final edited form as: Dev Dyn. 2012 Nov; 241(11): 1695–1707. Published online 2012 Sep 17. doi: 10.1002/dvdy.23857
PMCID:
PMC3760379
AbstractArticlePDF–5.5M
13.
Drosophila Myc Interacts with Host Cell Factor (dHCF) to Activate Transcription and Control Growth
Michael Furrer, Mirjam Balbi, Monica Albarca-Aguilera, Maria Gallant, Winship Herr, Peter Gallant
J Biol Chem. 2010 Dec 17; 285(51): 39623–39636. Published online 2010 Oct 11. doi: 10.1074/jbc.M110.140467
PMCID:
PMC3000943
AbstractArticlePDF–2.3M
14.
Novel Regulators of Planar Cell Polarity: A Genetic Analysis in Drosophila
Ursula Weber, William J. Gault, Patricio Olguin, Ekaterina Serysheva, Marek Mlodzik
Genetics. 2012 May; 191(1): 145–162. doi: 10.1534/genetics.111.137190
PMCID:
PMC3338256
AbstractArticlePDF–4.8M
15.
ATAC-king the complexity of SAGA during evolution
Gianpiero Spedale, H.Th. Marc Timmers, W.W.M. Pim Pijnappel
Genes Dev. 2012 Mar 15; 26(6): 527–541. doi: 10.1101/gad.184705.111
PMCID:
PMC3315114
AbstractArticlePDF–868K
16.
RNAseq analysis of the drug jian-yan-ling (JYL) using both in vivo and in vitro models
Xiaobo Zhang, Yunliang Zhai, Dandan Zhang, Chang Che, Yayun Zhang, Quan Li, Xue Zhang, Lingrui Zhao
Heliyon. 2023 May; 9(5): e16143. Published online 2023 May 19. doi: 10.1016/j.heliyon.2023.e16143
PMCID:
PMC10213199
AbstractArticlePDF–5.2M
17.
A Network of Conserved Damage Survival Pathways Revealed by a Genomic RNAi Screen
Dashnamoorthy Ravi, Amy M. Wiles, Selvaraj Bhavani, Jianhua Ruan, Philip Leder, Alexander J. R. Bishop
PLoS Genet. 2009 Jun; 5(6): e1000527. Published online 2009 Jun 19. doi: 10.1371/journal.pgen.1000527
Correction in:
PLoS Genet. 2009 Oct; 5(10): 10.1371/annotation/526db6e9-0ba5-4ec6-a257-2befb76f34b7.
PMCID:
PMC2688755
AbstractArticlePDF–1.6M
18.
Prediction and verification of microRNA targets by MovingTargets, a highly adaptable prediction method
Craig Burgler, Paul M Macdonald
BMC Genomics. 2005; 6: 88. Published online 2005 Jun 8. doi: 10.1186/1471-2164-6-88
PMCID:
PMC1180435
AbstractArticlePDF–495K
19.
Cell cycle-dependent and cell cycle-independent control of transcription by the Drosophila E2F/RB pathway
Dessislava K. Dimova, Olivier Stevaux, Maxim V. Frolov, Nicholas J. Dyson
Genes Dev. 2003 Sep 15; 17(18): 2308–2320. doi: 10.1101/gad.1116703
PMCID:
PMC196467
AbstractArticlePDF–496K
20.
A Genetic Screen and Transcript Profiling Reveal a Shared Regulatory Program for Drosophila Linker Histone H1 and Chromatin Remodeler CHD1
Harsh Kavi, Xingwu Lu, Na Xu, Boris A. Bartholdy, Elena Vershilova, Arthur I. Skoultchi, Dmitry V. Fyodorov
G3 (Bethesda) 2015 Apr; 5(4): 677–687. Published online 2015 Jan 27. doi: 10.1534/g3.115.016709
PMCID:
PMC4390582
AbstractArticlePDF–1.3M

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